Abstract
Congenital radioulnar synostosis is a rare skeletal defect associated with certain chromosomal abnormalities. We describe the first report of its occurrence in association with a pseudodicentric Y chromosome in a 27-year-old man with azoospermia and testicular dysfunction.
MeSH terms
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Adult
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Azoospermia / diagnostic imaging*
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Azoospermia / genetics
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Chromosomes, Human, Y*
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Humans
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Male
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Radiography
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Radius / abnormalities*
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Sex Chromosome Aberrations*
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Sex Chromosome Disorders / diagnostic imaging*
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Sex Chromosome Disorders / genetics
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Synostosis / diagnostic imaging*
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Synostosis / genetics
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Ulna / abnormalities*